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Guidewire - India CDSCO Medical Device Registration

Guidewire is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000780_6f79c5dae2a086e749af43b13df8e910_ecdc20657f6d5338897081b6423a7cb3. This device is marketed under the brand name Zipwire Hydrophilic Guidewire. The license holder is Boston Scientific India Pvt. Ltd.,, and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
Guidewire
UID: IMP/MD/2023/000780_6f79c5dae2a086e749af43b13df8e910_ecdc20657f6d5338897081b6423a7cb3

Brand Name

Zipwire Hydrophilic Guidewire

Device Class

Class B

Approving Authority

CDSCO

Product Information

The ZIPwire Hydrophilic Guidewire is intended to facilitate the placement of endourological instruments during diagnostic or interventional procedures. The ZIPwire Hydrophilic Guidewire is not intended for coronary artery, vascular or neurological use.

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